Lifeline VIEW 2 AUTO AED configuration

GUDID 10815098021526

DEFIBTECH, L.L.C.

Non-rechargeable public automated external defibrillator
Primary Device ID10815098021526
NIH Device Record Key3adaa607-3025-4fa5-8e6a-c7158f187d51
Commercial Distribution StatusIn Commercial Distribution
Brand NameLifeline VIEW 2 AUTO AED configuration
Version Model NumberDDU-2955
Company DUNS128340200
Company NameDEFIBTECH, L.L.C.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS110815098021526 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MKJAutomated External Defibrillators (Non-Wearable)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-12-17
Device Publish Date2025-12-09

Devices Manufactured by DEFIBTECH, L.L.C.

00815098021482 - Lifeline VIEW 22025-12-17
00815098021512 - Lifeline VIEW 2 Auto2025-12-17
00815098021536 - Lifeline ECG 22025-12-17
00815098021550 - DDU-29XX series, universal pad, single pair2025-12-17
10815098021496 - Lifeline VIEW 2 AED configuration2025-12-17
10815098021526 - Lifeline VIEW 2 AUTO AED configuration2025-12-17
10815098021526 - Lifeline VIEW 2 AUTO AED configuration2025-12-17
10815098021540 - Lifeline ECG 2 AED configuration2025-12-17
30815098021568 - Pads, DDU-29XX series, universal pad, 10 pairs2025-12-17
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